Run better, faster clinical trials with a functional service provider  

If you need to scale up operations, reduce costs or access specialised skills and knowledge that may not be available in-house, a functional service provider (FSP) can help.  

The FSP model gives sponsors greater flexibility when running clinical studies, enabling you to outsource specific components of a clinical trial. Our FSP solutions integrate with your internal processes and are tailored to your requirements, giving you specialised expertise where you need it most — without losing operational control. 

TMC originated from a consultancy background, so we’re well-placed to offer strategic planning and functional execution across regulatory affairs, clinical development, medical services, pharmacovigilance and quality assurance. 

Regulatory services  

Our comprehensive regulatory support accelerates your drug development process — from strategic planning to submission and post-approval compliance. 

We support your journey through global regulatory pathways, navigating efficiently from initial drug discovery through development, so you can avoid unnecessary delays and gain quicker approvals for clinical trials and marketing authorisations. 

Clinical development 

TMC aligns your clinical research strategy with regulatory and commercial goals, reducing delays, budget overruns and unnecessary protocol amendments. 

We support clinical study development and delivery across all trial phases globally, providing expert scientific and operational guidance throughout the drug development process to help you successfully deliver your clinical projects. 

Integrated medical services  

We have extensive clinical pre- and post-approval trial experience; our expertise covers writing and editing all types of documentation for internal and external company use, as well as regulatory submission, publication and marketing support. 

We bridge the gap between clinical development, regulatory compliance and market access, supporting you throughout your drug development programme to ensure your product not only meets safety and efficacy standards but is also optimised for commercial success. 

Pre– to post-approval pharmacovigilance  

We provide proactive pharmacovigilance guidance for the routine and ad hoc monitoring of the safety of your product, ensuring regulatory compliance from the first moment your drug is given to a patient and throughout its life cycle. 

Our pharmacovigilance and medical teams work closely together to provide a comprehensive suite of pre- and post-marketing services that ensure timely and accurate safety reporting — helping you protect your asset while making data-driven safety decisions to build trust with regulators and other stakeholders. 

Comprehensive quality assurance services 

Our experienced quality team gives you a clear picture of risk, ensuring compliance across your supply chain and maintaining high standards throughout the product life cycle. 

From one-off audits to becoming an integrated extension of your team, we offer a comprehensive range of flexible and scalable quality assurance services. 

If you want your new drug to reach patients faster and more efficiently, you need a functional service provider like TMC. Contact our team today to see how our specialised skills and knowledge help you scale and cut overheads when running clinical trials.